3057-69-0

Upstream product

• 1142-20-7 N-Cbz-Ala 
• 41036-19-5 L-alanyl-alanine methylester hydrochloride 
• 16012-70-7 benzyloxycarbonyl-L-alanyl-L-alanine 
• 2491-20-5 L-alanine methyl ester hydrochloride 
• 19794-10-6 (S)-methyl 2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)propanoate 

Downstream Products

• 73974-15-9 6-(Benzyloxycarbonyl-alanyl-alanyl-alanylamino)penicillansaeure 
• 5874-90-8 L-ala-L-ala-L-ala 
• 90058-03-0 H-Ala₅-OMe, HBr 
• 90058-02-9 H-Ala₅-OMe, HCl 
• 89595-83-5 Z-Ala₃-PheCH₂Cl 
• 90058-01-8 Z-Ala₅-OMe 
• 26910-17-8 N-acetyltri-L-alanyl methyl ester 
• 41036-27-5 H-Ala₃-OMe*HCl 
• 13585-98-3 N^α-benzyloxycarbobyl-L-alanyl-L-alanyl-L-alanine 

Relevant academic research and scientific papers

Fluorous Coupling Reagents: Application of 2-Chloro-4,6- bis[(heptadecafluorononyl)oxy]-1,3,5-triazine in Peptide Synthesis

Benzyloxycarbonyl N-protected and C-terminus methyl ester protected amino acids react in THF in the presence of 4-methylmorpholine and fluorous condensation reagent, 2-chloro-4,6-bis[(heptadecafluorononyl)oxy[-1,3,5- triazine, to form di- and tripeptides

Reaction of [(Cp2TiCH3)(THF)+] [BPh4-] with tripeptide derivatives: Formation of cationic (peptide)titanocene complexes

A series of Z- and Boc-protected tripeptide methyl esters [Z-/Boc-5 to -12(pept)] was prepared using the amino acids glycine, alanine and valine. In both the alanine and the valine series a single glycine unit was introduced and its position inside the tr

Thermitase - A Thermostable Serine Protease. I. Synthesis of Alanine Peptide Esters as Substrates of the Enzyme

The synthesis of N-acetylated and N-succinylated peptide esters of alanine is described.The peptides are built up from the Z-protected peptides by liquid phase fragment condensation and by acylation of the deprotected peptide esters.The kinetic parameters Km and kcat of some compounds are presented.